Phenylacetic Acid → HCID 11370967, compound

HRID 2053407Notes

Reaction equation

HRID 2053407 reaction equation
[C:1]1([CH2:7][C:8]([OH:10])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=O>>[Cl:18][C:15]1[CH:14]=[C:13]2[C:12](=[CH:17][CH:16]=1)[NH:11][C:8](=[O:10])[C:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)=[C:19]2[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1

Participants

3

Reactant 2

HCID 999Phenylacetic AcidHCID 128702-Amino-5-chlorobenzophenone

Product 1

HCID 11370967HCID 11370967, compoundYield 53%

Procedure

from phenylacetic acid and (2-amino-5-chloro-phenyl)-phenyl-methanone according to general procedure 2. Yield 53%.

Sources & evidence

ORD record
ord-e840e030d133404e816e51162ac59e5a
Source dataset
uspto-grants-2008_02
Patent number
US07326788B2

Reaction notes

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